Paclitaxel

Product NDC

0703-4767

11-digit product format

007034767

Labeler code

0703

Product ID

0703-4767_c4ff36a0-2a1f-48de-a7a2-2d643821c329

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Paclitaxel

Dosage form

INJECTION, SOLUTION, CONCENTRATE

Route

INTRAVENOUS

Labeler

Teva Parenteral Medicines, Inc.

Application

ANDA075184

Marketing category

ANDA

Marketing start

2008-10-23

Marketing end

2020-08-31

Substance

PACLITAXEL

Active strength

6 mg/mL

Pharmacologic classes

Microtubule Inhibition [PE],Microtubule Inhibitor [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record